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81.
J. A. RAVEN 《Plant, cell & environment》1997,20(2):147-154
A testable mechanism of CO2 accumulation in photolithotrophs, originally suggested by Pronina & Semenenko, is quantitatively analysed. The mechanism involves (as does the most widely accepted hypothesis) the delivery of HCO3? to the compartment containing Rubisco. It differs in proposing subsequent HCO3? entry (by passive uniport) to the thylakoid lumen, followed by carbonic anhydrase activity in the lumen; uncatalysed conversion of HCO3? to CO2, even at the low pH of the lumen, is at least 300 times too slow to account for the rate of inorganic C acquisition. Carbonic anhydrase converts the HCO3? to CO2 at the lower pH maintained in the illuminated thylakoid lumen by the light-driven H+ pump, generating CO2 at 10 times or more the thylakoid HCO3? concentration. Efflux of this CO2 can suppress Rubisco oxygenase activity and stimulate carboxylase activity in the stroma. This mechanism differs from the widely accepted hypotheses in the required location of carbonic anhydrase, i.e. in the thylakoid lumen rather than the stroma or pyrenoid, and in the need for HCO3? influx to thylakoids. The capacity for anion (assayed as Cl?) entry by passive uniport reported for thylakoid membranes is adequate for the proposed mechanism; if the Cl? channel does not transport HCO3?, HCO3? entry could be by combination of the Cl? channel with a Cl? HCO3? antiporter. This mechanism is particularly appropriate for organisms which lack overt accumulation of total inorganic C in cells, but which nevertheless have the gas exchange characteristics of an organism with a CO2-concentrating mechanism. 相似文献
82.
83.
人类细胞色素P450与药物氧化代谢遗传多态性分子机制的研究现状 总被引:10,自引:0,他引:10
近年,在表型及基因型上均发现存在药物氧化代谢多态性,特别是对于人类细胞色素P450氧化酶与药氧化代谢遗传多态性的关系进行了深入的研究。有关CYP2D6、CYP2C19等的突变已大多被鉴定;CYP1A1、CYP1A2等在表型存在多态性而确切的遗传机制尚不清楚。 相似文献
84.
Gordon C. K. Roberts 《Neurochemical research》1996,21(9):1117-1124
NMR spectroscopy has proved to be a valuable tool in the study of the interactions between enzymes and their substrates. The
kinds of structural and dynamic information which can be obtained are illustrated by studies of three enzymes involved in
drug metabolism. Cytochromes P450 play a crucial role in metabolism of a wide range of exogenous chemicals. NMR has been used to measure distances from the
haem iron of the cytochrome to protons of the bound substrate, leading to detailed structural models for the enzyme-substrate
complexes. The other two enzymes, chloramphenicol acetyltransferase and β-lactamase, are responsible for bacterial resistance
to specific antibiotics. In chloramphenicol acetyltransferase, NMR has been used to determine the conformation of coenzyme
A bound to the enzyme, while in the case of β-lactamase the pK of a specific lysine residue at the active site has been determined,
providing valuable information on the catalytic mechanism.
Special issue dedicated to Dr. Herman Bachelard. 相似文献
85.
Substituted enzyme (or ping-pong) mechanisms usually involve enzymes that exist in two forms that alternate during the catalytic
reaction. A method is described here for determining the position of the equilibrium of a half reaction in a ping-pong enzyme
mechanism that is based on the kinetics of the burst reaction which occurs upon addition of reactants that recycle the enzyme
from one form to another. The theoretical basis for the analysis is developed, and the method is applied to the half reaction
of the aldimine form of aspartate transaminase with difluoro-oxaloacetate.
Special issue dedicated to Herman Bachelard 相似文献
86.
This study examined the localized action of neuropeptide Y (NPY) on monoamine transmitter activity in the hypothalamus of
the unrestrained rat as this peptide induced hypothermia, spontaneous feeding or both responses simultaneously. A guide tube
was implanted in the anterior hypothalamic pre-optic area (AH/POA) of Sprague-Dawley rats. Then either control CSF vehicle
or NPY in a dose of either 100 ng/μl or 250 ng/μl was perfused by push-pull cannulae in this structure in the fully sated,
normothermic rat. Successive perfusions were carried out at a rate of 20 μl/min for 6.0 min with an interval of 6.0 min elapsing
between each. Samples of perfusate were assayed by HPLC for their levels of dopamine (DA), norepinephrine (NE), serotonin
(5-HT) and their respective metabolites. Whereas control CSF was without effect on body temperature (Tb) or feeding, repeated perfusions of NPY over 3.0 hr caused dose—dependent eating from 4 to 39 g of food, hypothermia of 0.9
to 2.3°C or both responses concurrently. As the rats consumed 11–39 g of food, the efflux of NE, MHPG, DOPAC and 5-HT was
enhanced significantly, whereas during the fall in Tb the efflux of NE, DOPAC and 5-HIAA from the AH/POA increased. When the Tb of the rat declined simultaneously with eating behavior, the levels in perfusate of DOPAC and HVA increased significantly
while MHPG declined. During perfusion of the AH/POA with NPY the turnover of NE declined while DA and 5-HT turnover increased
during hypothermia alone or when accompanied by feeding. These results demonstrate that the sustained elevation in NPY within
the AH/POA causes a selective alteration in the activity of the neurotransmitters implicated in thermoregulation, satiety
and hunger. These findings suggest that both DA and NE comprise intermediary factors facilitating the action of NPY on neurons
involved in thermoregulatory and ingestive processes. The local activity of NPY on hypothalamic neurons apparently shifts
the functional balance of serotonergic and catecholaminergic neurons now thought to play a primary role in the control of
energy metabolism and caloric intake. 相似文献
87.
Ricardo O. Louro Teresa Catarino Carlos A. Salgueiro Jean LeGall António V. Xavier 《Journal of biological inorganic chemistry》1996,1(1):34-38
Using potentiometric titrations, two protons were found to participate in the redox-Bohr effect observed for cytochrome c
3 from Desulfovibrio vulgaris (Hildenborough). Within the framework of the thermodynamic model previously presented, this finding supports the occurrence
of a concerted proton-assisted 2e– step, ideally suited for the coupling role of cytochrome c
3 to hydrogenase. Furthermore, at physiological pH, it is shown that when sulfate-reducing bacteria use H2 as energy source, cytochrome c
3 can be used as a charge separation device, achieving energy transduction by energising protons which can be left in the acidic
periplasmic side and transferring deenergised electrons to sulfate respiration. This mechanism for energy transduction, using
a full thermodynamic data set, is compared to that put forward to explain the proton-pumping function of cytochrome c oxidase. 相似文献
88.
D. Buffard R. Esnault Á. Kondorosi 《World journal of microbiology & biotechnology》1996,12(2):175-188
During effective symbiosis, rhizobia colonize their hosts, and avoid plant defence mechanisms. To determine whether the host defence responses can be elicited by the symbiotic bacteria, specific markers involved in incompatible pathogenic interactions are required. The available markers of alfalfa defence mechanisms are described and their use in the study of the symbiotic interaction discussed. As defence-related gene expression in roots is not always related to defence mechanisms, other model systems have been established allowing confirmation of an important role of bacterial surface components in alfalfa-Rhizobium meliloti interactions. Nod factors at high concentrations have been shown to elicit defence-like responses in Medicago cell suspensions and roots. Elicitation of defence mechanisms by high levels of Nod factors in Rhizobium-infected roots may be a part of the mechanism by which nodulation is feed-back regulated.The authors are with the Institut des Sciences Végétales, CNRS, F-91198 Gif-sur-Yvette cédex, France. 相似文献
89.
The increasing resistance of pathogens to common antibiotics, as well as the need to control urease activity to improve the yield of soil nitrogen fertilization in agricultural applications, has stimulated the development of novel classes of molecules that target urease as an enzyme. In this context, the newly developed compounds on the basis of 1-heptanoyl-3-arylthiourea family were evaluated for Jack bean urease enzyme inhibition activity to validate their role as potent inhibitors of this enzyme. 1-Heptanoyl-3-arylthioureas were obtained in excellent yield and characterized through spectral and elemental analysis. All the compounds displayed remarkable potency against urease inhibition as compared to thiourea standard. It was found that novel compounds fulfill the criteria of drug-likeness by obeying Lipinski’s rule of five. Particularly compound 4a and 4c can serve as lead molecules in 4D (drug designing discovery and development). Kinetic mechanism and molecular docking studies also carried out to delineate the mode of inhibition and binding affinity of the molecules. 相似文献
90.